FDA approves Ascendis Pharma’s once-weekly YUVIWEL for children with achondroplasia aged 2 and older

Reuters
02/28
FDA approves Ascendis Pharma’s once-weekly YUVIWEL for children with achondroplasia aged 2 and older

Ascendis Pharma A/S said the U.S. Food and Drug Administration granted accelerated approval for YUVIWEL (navepegritide), a once-weekly treatment indicated to increase linear growth in children aged 2 years and older with achondroplasia with open epiphyses. The company said continued approval may be contingent on confirmatory trials, and that the FDA also issued a Rare Pediatric Disease Priority Review Voucher in connection with the approval. Ascendis expects commercial availability in the United States in the early part of the second quarter of 2026.

Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Ascendis Pharma A/S published the original content used to generate this news brief via GlobeNewswire (Ref. ID: 202602271757PRIMZONEFULLFEED9663256) on February 27, 2026, and is solely responsible for the information contained therein.

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